ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.664+1G>A

dbSNP: rs61811105
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000664952 SCV000788996 likely pathogenic Glycogen storage disease type III 2017-01-05 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000664952 SCV003816686 pathogenic Glycogen storage disease type III 2023-01-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000664952 SCV004049927 likely pathogenic Glycogen storage disease type III 2023-04-11 criteria provided, single submitter clinical testing

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